Clinical Development Jobs In China - 741 Job Positions Available

1 – 20 of 741 jobs
Novotech jobs

Minimum Qualifications & Experience: Required Bachelors degree or equivalent in medicine, pharmacy, biology, or another related life science discipline. Minimum 10 years of experience within clinical research, drug development, or CRO environments. Demonstrated understanding of Phase I and

Novotech  25 days ago
Philips jobs

Job TitleClinical Development Scientist CT Job Description Job title: In this role, you will leverage your clinical and technical expertise to drive the development and growth of Philips CT business strategies. You will play a key role in shaping

Philips  22 days ago
Philips jobs

Job TitleIntern - Clinical Development Assistant Job Description Job Description Job Responsibilities: According to the project plan and time requirements, work in the office or remotely, mainly completing the following tasks: 1. Manage and maintain the teams clinical evidence

Philips  10 days ago
BioNTech SE jobs

Shanghai, China | full time | Job ID: 9282 Your main responsibilities are: Participate in the design and execution of clinical trials of their assigned programs, helping to create the clinical development plan for new compounds, and pave a

BioNTech SE  8 days ago
Philips jobs

Job TitleClinical Development Scientist, Ultrasound &EI Job Description In this role, you have the opportunity to Be a member of the medical and clinical affairs team in Greater China. Medical and Clinical affairs team is an integral part of

Philips  2 days ago
Roche jobs

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,

Roche  11 days ago
ICON plc jobs

Clinical Research Associate II, China ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are

ICON Plc  12 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Purpose: The Associate Director, Scientific Development supports and leads assigned customer- and commercial-focused strategic development engagements that accelerate business growth, customer impact, and coordinated scientific solutioning. This role connects customer needs,

Thermo Fisher Scientific  12 days ago
Caidya jobs

Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference

Caidya  11 days ago
Novotech jobs

Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of

Novotech  12 days ago
Novotech jobs

Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of

Novotech  12 days ago
Philips jobs

Job TitleAdvisory MR Clinical Scientist Job Description Your role: Collaborate with radiologists to conduct clinical application research on MR / AI, participate in the design of scientific research projects, follow-up on progress, contribute to SCI paper writing and

Philips  12 days ago
Novotech jobs

Responsible for day-to-day data processing operations for data management projects, including CRF (or other study data document) tracking, entry, and filing. Provides administrative and project management support to CDMs for data management projects as required, including

Novotech  26 days ago
IQVIA jobs

Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮:线上测评 完成指定的线上测试,用于初步筛选。 第二轮:业务面试 与业务部门进行面谈,深入了解您的专业背景与职位匹配度。 第三轮:结果通知 招聘团队将在流程结束后,正式告知最终结果。 Essential Functions • Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well

IQVIA  26 days ago
IQVIA jobs

Job Overview Provides administrative and/or technical support. Recruitment Process 第一轮:线上测评 完成指定的线上测试,用于初步筛选。 第二轮:业务面试 与业务部门进行面谈,深入了解您的专业背景与职位匹配度。 第三轮:结果通知 招聘团队将在流程结束后,正式告知最终结果。 Essential Functions • Responsible to reconcile SAP Grant Payment Report to Excel Grant Payment Report for assigned Sponsors’ studies, as well

IQVIA  26 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our

Thermo Fisher Scientific  25 days ago
Takeda jobs

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms

Takeda  25 days ago
ICON plc jobs

ICON- Clinical Trial Manager -Shanghai ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are

ICON Plc  25 days ago
Boehringer Ingelheim jobs

About Human Pharmaceutical Business With global presence, Boehringer Ingelheim has industry-leading expertise in medicine research and development. We are constantly developing the next generation of medical breakthroughs and successfully delivering innovations to meet the medical needs of

Boehringer Ingelheim  23 days ago
Caidya jobs

Job Overview: The Senior Clinical Research Associate monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Company and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference

Caidya  24 days ago

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